Overview

Variant ID 9488
Entrez Gene ID 114781
Gene BTBD9 (GeneCards)
Location hg19 6:38310132-38310132
hg38 6:38342356-38342356
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000006.11:g.38310132 C>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.5047
CADD Raw score (version 1.3) -0.121509 (Deleterious)
FATHMM raw prediction score 0.04859 (Tolerated)
Deleterious probability by DeFine 0.0834 (Neutral)
Entrez Gene ID 114781 (NCBI Gene)
Official Gene Symbol BTBD9 (GeneCards)
Number of variants in BTBD9 in this database 8 (view all the variants)
Full name BTB domain containing 9
Band 6p21.2
Other IDs Vega: OTTHUMG00000014634
OMIM: 611237
HGNC: HGNC:21228
Ensembl: ENSG00000183826
Other names dJ322I12.1
Summary This locus encodes a BTB/POZ domain-containing protein. This domain is known to be involved in protein-protein interactions. Polymorphisms at this locus have been reported to be associated with susceptibility to Restless Legs Syndrome and may also be associated with Tourette Syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2011]

Individual #1

Individual ID 29217584.10 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;